n14162025
type | n |
lex_filenum | 26 |
def | a disease caused by a dominant mutant gene on an autosome |
Outgoing links | |
Hypernym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
Hyponym | Huntington's chorea, Huntington's disease; malignant hyperthermia; Marfan's syndrome; neurofibromatosis, von Recklinghausen's disease; osteogenesis imperfecta |
Incoming links | |
Hyponym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
Hypernym | Huntington's chorea, Huntington's disease; malignant hyperthermia; Marfan's syndrome; neurofibromatosis, von Recklinghausen's disease; osteogenesis imperfecta |
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